Emulsion aggregation, developer, and method of making the same

ABSTRACT

A polyester toner includes particles of a resin, a colorant, an optional wax, and a polyion coagulant, where the toner is prepared by an emulsion aggregation process.

BACKGROUND

This present disclosure relates to toners and developers containing thetoners for use in forming and developing images, and in particular topolyester emulsion/aggregation toners formed using polyions ascoagulants. The disclosure also relates to processes for producing andusing such toners and developers.

Emulsion aggregation toners are excellent toners to use in forming printand/or xerographic images in that the toners can be made to have uniformsizes and in that the toners are environmentally friendly. U.S. patentsdescribing emulsion aggregation toners include, for example, U.S. Pat.Nos. 5,370,963, 5,418,108, 5,290,654, 5,278,020, 5,308,734, 5,344,738,5,403,693, 5,364,729, 5,346,797, 5,348,832, 5,405,728, 5,366,841,5,496,676, 5,527,658, 5,585,215, 5,650,255, 5,650,256, 5,501,935,5,723,253, 5,744,520, 5,763,133, 5,766,818, 5,747,215, 5,827,633,5,853,944, 5,804,349, 5,840,462, and 5,869,215, the entire disclosuresof which are incorporated herein by reference.

Two main types of emulsion aggregation toners are known. First is anemulsion aggregation process that forms acrylate based, e.g., styreneacrylate, toner particles. See, for example, U.S. Pat. No. 6,120,967,the entire disclosure of which is incorporated herein by reference, asone example of such a process. Second is an emulsion aggregation processthat forms polyester, e.g., sodio sulfonated polyester, toner particles.See, for example, U.S. Pat. No. 5,916,725, the entire disclosure ofwhich is incorporated herein by reference, as one example of such aprocess.

Emulsion aggregation techniques typically involve the formation of anemulsion latex of the resin particles, which particles have a small sizeof from, for example, about 5 to about 500 nanometers in diameter, byheating the resin, optionally with solvent if needed, in water, or bymaking a latex in water using an emulsion polymerization. A colorantdispersion, for example of a pigment dispersed in water, optionally alsowith additional resin, is separately formed. The colorant dispersion isadded to the emulsion latex mixture, and an aggregating agent orcomplexing agent is then added to form aggregated toner particles. Theaggregated toner particles are heated to enable coalescence/fusing,thereby achieving aggregated, fused toner particles.

Addition of a coagulant during the emulsion/aggregation process is animportant step, to assist in aggregation of the primary polymer,colorant, and the like particles. For example, U.S. Pat. No. 6,120,967,mentioned above, describes a process where styrene acrylate-based resinsare used to form toner particles, and in which a cationic coagulant suchas poly-aluminum chloride, aluminum sulfate, zinc sulfate, alum, anddialkyl benzenealkyl ammonium chloride is used as the coagulant.However, different coagulants are used in polyester-based resinemulsion/aggregation processes. For example, U.S. Pat. No. 5,916,725,also mentioned above, describes a process where polyester-based resinsare used to form toner particles, and in which the coagulant is a smallorganic amine, such as 2-methyl-1,5-pentanediamine.

In other polyester-based resin emulsion/aggregation processes, zincacetate has been extensively used as a coagulant. See, for example, U.S.Pat. Nos. 6,500,597, 6,743,559, and 6,756,176, which disclose the use ofmetal salts, such as aluminum sulfate, aluminum chloride, zinc sulfate,magnesium sulfate, magnesium chloride, potassium-aluminum sulfate, orzinc acetate, as coagulants for producing polyester toners inemulsion/aggregation processes.

However, a problem exists with the use of such metal salts as zincacetate in producing polyester toners. In particular, only a smallproportion of the zinc acetate, about 2 to 3 weight %, gets incorporatedinto the toner particles. The remaining zinc acetate is in the aqueousphase, and must be filtered and separated before the aqueous phase canbe discharged into the environment. This separation thus adds asignificant cost to the toner production and waste disposal. The lowrate of incorporation of zinc acetate into the toner particles isbelieved to be primarily due to its high solubility in water and thepartial dissociation of the zinc acetate However, coagulants such aspolyions have not previously been used in producing polyester toners,such as sulfonated polyester toners, because the sulfonate groups on thepolyester resin particles are not sufficient to provide a controlledaggregation or coalescence in the presence of the more active polyioncoagulants.

Accordingly, there is a need in the art for improved emulsionaggregation toner processes, particularly for use with polyester tonerparticles, that provide an efficient, controlled process withoutincreasing the separation and disposal costs.

SUMMARY

The present disclosure addresses these and other needs, by providingimproved coagulants and processes for making polyesteremulsion/aggregation toner compositions. The disclosure provides moreefficient coagulant materials, in that a higher amount of the coagulantis incorporated into the aggregated toner particles, thereby improvingprocess efficiency, reducing process cost, and reducing wasteprocessing.

In embodiments, the present disclosure provides a toner comprisingparticles of a resin, a colorant, an optional wax, and a polyioncoagulant, wherein said toner is prepared by an emulsion aggregationprocess.

In another embodiment, the present disclosure provides a process forpreparing a toner, comprising:

mixing a resin emulsion, a colorant dispersion, and an optional wax toform a mixture;

adding an organic or an inorganic acid to said mixture;

adding a polyion coagulant to said mixture;

heating the mixture, permitting aggregation and coalescence of saidresin and colorant, and optionally cooling the mixture and isolating theproduct,

wherein the polyion coagulant is added to said mixture at least one ofbefore or during said heating.

In embodiments, the present disclosure also provides methods for makingdevelopers incorporating such toners, as well as development processesusing the toners and developers.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

The toner of the present disclosure is comprised of toner particlescomprised of at least a latex emulsion polyester polymer resin and acolorant dispersion. The toner particles may also include at least a waxdispersion and other conventional optional additives, such as colloidalsilica (as a flow agent) and the like. The toner is made using a polyionas a coagulant during the aggregation phase of the process.

The specific latex for resin, polymer or polymers selected for the tonerof the present disclosure include polyester and/or its derivatives,including polyester resins and branched polyester resins, polyimideresins, branched polyimide resins, poly(styrene-acrylate)resins,crosslinked poly(styrene-acrylate)resins,poly(styrene-methacrylate)resins, crosslinkedpoly(styrene-methacrylate)resins, poly(styrene-butadiene)resins,crosslinked poly(styrene-butadiene)resins, alkali sulfonated-polyesterresins, branched alkali sulfonated-polyester resins, alkalisulfonated-polyimide resins, branched alkali sulfonated-polyimideresins, alkali sulfonated poly(styrene-acrylate)resins, crosslinkedalkali sulfonated poly(styrene-acrylate)resins,poly(styrene-methacrylate)resins, crosslinked alkalisulfonated-poly(styrene-methacrylate)resins, alkalisulfonated-poly(styrene-butadiene) resins, crosslinked alkali sulfonatedpoly(styrene-butadiene)resins, and the like. In an embodiment, forexample, a particularly referred resin is a polyester, such as asulfonated polyester.

Illustrative examples of polymer resins selected for the process andparticles of the present disclosure include any of the variouspolyesters, such as polyethylene-terephthalate,polypropylene-terephthalate, polybutylene-terephthalate,polypentylene-terephthalate, polyhexalene-terephthalate,polyheptadene-terephthalate, polyoctalene-terephthalate,polyethylene-sebacate, polypropylene sebacate, polybutylene-sebacate,polyethylene-adipate, polypropylene-adipate, polybutylene-adipate,polypentylene-adipate, polyhexalene-adipate, polyheptadene-adipate,polyoctalene-adipate, polyethylene-glutarate, polypropylene-glutarate,polybutylene-glutarate, polypentylene-glutarate, polyhexalene-glutarate,polyheptadene-glutarate, polyoctalene-glutarate polyethylene-pimelate,polypropylene-pimelate, polybutylene-pimelate, polypentylene-pimelate,polyhexalene-pimelate, polyheptadene-pimelate, poly(propoxylatedbisphenol-fumarate), poly(propoxylated bisphenol-succinate),poly(propoxylated bisphenol-adipate), poly(propoxylatedbisphenol-glutarate), SPAR™ (Dixie Chemicals), BECKOSOL™ (ReichholdChemical Inc), ARAKOTE™ (Ciba-Geigy Corporation), HETRON™ (AshlandChemical), PARAPLEX™ (Rohm & Hass), POLYLITE™ (Reichhold Chemical Inc),PLASTHALL™ (Rohm & Hass), CYGAL™ (American Cyanamide), ARMCO™ (ArmcoComposites), ARPOL™ (Ashland Chemical), CELANEX™ (Celanese Eng), RYNITE™(DuPont), STYPOL™ (Freeman Chemical Corporation) mixtures thereof andthe like. The resins can also be functionalized, such as carboxylated,sulfonated, or the like, and particularly such as sodio sulfonated, ifdesired.

In embodiments, a sulfonated polyester resin such as a sodio sulfonatedpolyester resin is preferred. When used, the sulfonated polyester resincan have any desired degree of sulfonation. For example, the sulfonationdegree can be from about 0.1 to about 20 percent, such as from about 0.3to about 6 percent.

The latex polymer may be present in an amount of from about 70 to about95% by weight of the toner particles (i.e., toner particles exclusive ofexternal additives) on a solids basis, such as from about 75 to about85% by weight of the toner. However, amounts outside of these ranges canbe used, in embodiments, depending upon the type and amounts of othermaterials present.

The monomers used in making the selected polymer are not limited, andthe monomers utilized may include any one or more of, for example,ethylene, propylene, and the like. Known chain transfer agents, forexample dodecanethiol or carbon tetrabromide, can be utilized to controlthe molecular weight properties of the polymer. Any suitable method forforming the latex polymer from the monomers may be used withoutrestriction.

Various suitable colorants can be employed in toners of the presentdisclosure, including suitable colored pigments, dyes, and mixturesthereof, including carbon black, such as REGAL 330 carbon black,acetylene black, lamp black, aniline black, Chrome Yellow, Zinc Yellow,SICOFAST Yellow, SUNBRITE Yellow, LUNA Yellow, NOVAPERM Yellow, ChromeOrange, BAYPLAST Orange, Cadmium Red, LITHOL Scarlet, HOSTAPERM Red,FANAL PINK, HOSTAPERM Pink, LUPRETON Pink, LITHOL Red, RHODAMINE Lake B,Brilliant Carmine, HELIOGEN Blue, HOSTAPERM Blue, NEOPAN Blue, PV FastBlue, CINQUASSI Green, HOSTAPERM Green, titanium dioxide, cobalt,nickel, iron powder, SICOPUR 4068 FF, and iron oxides such as MAPICOBlack (Columbia) NP608 and NP604 (Northern Pigment), BAYFERROX 8610(Bayer), M08699 (Mobay), TMB-100 (Magnox), mixtures thereof and thelike.

The colorant, such as carbon black, cyan, magenta and/or yellowcolorant, is incorporated in an amount sufficient to impart the desiredcolor to the toner. In general, pigment or dye is employed in an amountranging from about 2% to about 35% by weight of the toner particles on asolids basis, such as from about 5% to about 25% by weight or from about5 to about 15% by weight. However, amounts outside these ranges can alsobe used, in embodiments.

Of course, as the colorants for each color are different, the amount ofcolorant present in each type of color toner typically is different. Forexample, in some embodiments of the present disclosure, a cyan toner mayinclude about 3 to about 11% by weight of colorant (such as Pigment Blue15:3 from SUN), a magenta toner may include about 3 to about 15% byweight of colorant (such as Pigment Red 122, Pigment Red 185, PigmentRed 238, and/or mixtures thereof), a yellow toner may include about 3 toabout 10% by weight of colorant (such as Pigment Yellow 74), and a blacktoner may include about 3 to about 10% by weight of colorant (such ascarbon black).

In addition to the latex polymer binder and the colorant, the toners ofthe present disclosure may also optionally contain a wax, typicallyprovided in a wax dispersion, which wax dispersion can be of a singletype of wax or a mixture of two or more preferably different waxes. Asingle wax can be added to toner formulations, for example, to improveparticular toner properties, such as toner particle shape, presence andamount of wax on the toner particle surface, charging and/or fusingcharacteristics, gloss, stripping, offset properties, and the like.Alternatively, a combination of waxes can be added to provide multipleproperties to the toner composition.

When a wax dispersion is used, the wax dispersion can include any of thevarious waxes conventionally used in emulsion aggregation tonercompositions. Suitable examples of waxes include, but are not limitedto, polyethylene, polypropylene, polyethylene/amide,polyethylenetetrafluoroethylene, andpolyethylenetrtraflouorethylene/amide. Other examples include, forexample, polyolefin waxes, such as polyethylene waxes, including linearpolyethylene waxes and branched polyethylene waxes, and polypropylenewaxes, including linear polypropylene waxes and branched polypropylenewaxes; paraffin waxes; Fischer-Tropsch waxes; amine waxes; siliconewaxes; mercapto waxes; polyester waxes; urethane waxes; modifiedpolyolefin waxes (e.g., a carboxylic acid-terminated polyethylene wax ora carboxylic acid-terminated polypropylene wax); amide waxes, such asaliphatic polar amide functionalized waxes; aliphatic waxes consistingof esters of hydroxylated unsaturated fatty acids; high acid waxes, suchas high acid montan waxes; microcrystalline waxes, such as waxes derivedfrom distillation of crude oil; and the like. By “high acid waxes” it ismeant a wax material that has a high acid content. The waxes can becrystalline or non-crystalline, as desired, although crystalline waxesare preferred, in embodiments. By “crystalline polymeric waxes” it ismeant that a wax material contains an ordered array of polymer chainswithin a polymer matrix that can be characterized by a crystallinemelting point transition temperature, Tm. The crystalline meltingtemperature is the melting temperature of the crystalline domains of apolymer sample. This is in contrast to the glass transition temperature,Tg, which characterizes the temperature at which polymer chains begin toflow for the amorphous regions within a polymer.

To incorporate the wax into the toner, it is preferable for the wax tobe in the form of one or more aqueous emulsions or dispersions of solidwax in water, where the solid wax particle size is usually in the rangeof from about 100 to about 500 nm.

The toners may contain the wax in any amount of from, for example, about3 to about 15% by weight of the toner, on a dry basis. For example, thetoners can contain from about 5 to about 11% by weight of the wax.

The toners of the present disclosure may also contain a coagulant. Avariety of coagulants are known in the art, as described above. However,the disclosure relates to the specific selection of polyions, ormultivalent ions, as coagulants in forming the toner compositions. Asused herein, “polyion coagulant” refers to a coagulant that is a salt oroxide, preferably a metal salt or metal oxide, formed from a metalspecies having a valence of at least 3, and preferably at least 4 or 5.Suitable coagulants thus include, for example, coagulants based onaluminum such as polyaluminum halides such as polyaluminum fluoride andpolyaluminum chloride (PAC), polyaluminum silicates such as polyaluminumsulfosilicate (PASS), polyaluminum hydroxide, polyaluminum phosphate,and the like. Other suitable coagulants include, but are not limited to,tetraalkyl titinates, dialkyltin oxide, tetraalkyltin oxide hydroxide,dialkyltin oxide hydroxide, aluminum alkoxides, alkylzinc, dialkyl zinc,zinc oxides, stannous oxide, dibutyltin oxide, dibutyltin oxidehydroxide, tetraalkyl tin, and the like. Such polyion coagulants mayhave any desired number of polyion atoms present. For example, preferredpolyaluminum compounds in embodiments have from about 2 to about 13,such as from about 3 to about 8, aluminum ions present in the compound

Such polyion coagulants are preferred, in embodiments, because they aremore highly incorporated into the toner particles during particleaggregation, and thus less of the coagulant remains in solutionrequiring extra subsequent waste processing. For example, inembodiments, at least about 50%, such as at least about 75% or at leastabout 80% by weight of the polyion coagulant is incorporated into thetoner particles during particle aggregation, meaning that less thanabout 50%, such as less than about 25% or less than about 20%,respectively, of the coagulant remains in solution after completion ofparticle aggregation. In one embodiment, as high as about 90% or more ofthe polyion coagulant is incorporated into the toner particles duringparticle aggregation, meaning that less than about 10% of the coagulantremains in solution after completion of particle aggregation.

The coagulant is present in the toner particles, exclusive of externaladditives and on a dry weight basis, in amounts of from 0 to about 5% byweight of the toner particles, such as from about greater than 0 toabout 3% by weight of the toner particles.

The toner may also include additional known positive or negative chargeadditives in effective suitable amounts of, for example, from about 0.1to about 5 weight percent of the toner, such as quaternary ammoniumcompounds inclusive of alkyl pyridinium halides, bisulfates, organicsulfate and sulfonate compositions such as disclosed in U.S. Pat. No.4,338,390, cetyl pyridinium tetrafluoroborates, distearyl dimethylammonium methyl sulfate, aluminum salts or complexes, and the like.

Also, in preparing the toner by the emulsion aggregation procedure, oneor more surfactants may be used in the process. Suitable surfactantsinclude anionic, cationic and nonionic surfactants. In embodiments, theuse of anionic and nonionic surfactants are preferred to help stabilizethe aggregation process in the presence of the polyion coagulant, whichotherwise could lead to aggregation instability.

Anionic surfactants include sodium dodecylsulfate (SDS), sodium dodecylbenzene sulfonate, sodium dodecylnaphthalene sulfate, dialkylbenzenealkyl, sulfates and sulfonates, abitic acid, and the NEOGEN brandof anionic surfactants. An example of a suitable anionic surfactant isNEOGEN RK available from Daiichi Kogyo Seiyaku Co. Ltd., or TAYCA POWERBN2060 from Tayca Corporation (Japan), which consists primarily ofbranched sodium dodecyl benzene sulphonate.

Examples of cationic surfactants include dialkyl benzene alkyl ammoniumchloride, lauryl trimethyl ammonium chloride, alkylbenzyl methylammonium chloride, alkyl benzyl dimethyl ammonium bromide, benzalkoniumchloride, cetyl pyridinium bromide, C₁₂, C₁₅, C₁₇ trimethyl ammoniumbromides, halide salts of quatemized polyoxyethylalkylamines, dodecylbenzyl triethyl ammonium chloride, MIRAPOL and ALKAQUAT available fromAlkaril Chemical Company, SANISOL (benzalkonium chloride), availablefrom Kao Chemicals, and the like. An example of a suitable cationicsurfactant is SANISOL B-50 available from Kao Corp., which consistsprimarily of benzyl dimethyl alkonium chloride.

Examples of nonionic surfactants include polyvinyl alcohol, polyacrylicacid, methalose, methyl cellulose, ethyl cellulose, propyl cellulose,hydroxy ethyl cellulose, carboxy methyl cellulose, polyoxyethylene cetylether, polyoxyethylene lauryl ether, polyoxyethylene octyl ether,polyoxyethylene octylphenyl ether, polyoxyethylene oleyl ether,polyoxyethylene sorbitan monolaurate, polyoxyethylene stearyl ether,polyoxyethylene nonylphenyl ether, dialkylphenoxy poly(ethyleneoxy)ethanol, available from Rhone-Poulenc Inc. as IGEPAL CA-210, IGEPALCA-520, IGEPAL CA-720, IGEPAL CO-890, IGEPAL CO-720, IGEPAL CO-290,IGEPAL CA-210, ANTAROX 890 and ANTAROX 897. An example of a suitablenonionic surfactant is ANTAROX 897 available from Rhone-Poulenc Inc.,which consists primarily of alkyl phenol ethoxylate.

Any suitable emulsion aggregation procedure may be used in forming theemulsion aggregation toner particles without restriction. Theseprocedures typically include the basic process steps of at leastaggregating an emulsion containing binder, one or more colorants, one ormore surfactants, a polyion coagulant, optionally a wax emulsion, andone or more additional optional additives to form aggregates,subsequently coalescing or fusing the aggregates, and then recovering,optionally washing and optionally drying the obtained emulsionaggregation toner particles.

In an embodiment, the process comprises mixing a polyester-based resinemulsion with a colorant in the presence of a polyion coagulant, an acidand one or more surfactants, and thereafter heating the mixtureresulting in metal ions generated from the reaction between the polyioncoagulant and the acid to effect aggregation/coalescence of the emulsionparticles and colorant to form coalesced toner particles of resin andcolorant.

An exemplary process for producing the toner particles comprises thefollowing steps.

First, an emulsion latex is provided (or generated), comprised ofpolyester-based resin particles, such as sodio sulfonated polyesterresin particles. The latex is preferably heated in water to atemperature of, for example, from about 65° C. to about 90° C.

Second, a colorant dispersion is added, preferably with shearing, to theresin latex. The colorant dispersion can comprise, for example, fromabout 20 to about 50 percent of a predispersed colorant in water. Anorganic or an inorganic acid, and one or more surfactants, are alsoadded to the mixture of the resin and colorant dispersions. If desired,the mixture can be heated to a desired temperature in preparation for asubsequent aggregation reaction, such as a temperature of from about 45°C. to about 65° C. Other optional additives and/or dispersions can alsobe included, such as a wax dispersion, a second or additional resindispersion, and the like. The shearing can be conducted, for example, byhomogenizing at from about 1,000 revolutions per minute to about 10,000revolutions per minute, at a temperature of from about 25° C. to about35° C., and for a duration of from about 1 minute to about 120 minutes.As desired, the mixture can also comprise other components, such as anoptional wax, and the like.

Third, a polyion coagulant, as described above, is added to the mixture.The polyion coagulant, which is preferably water insoluble, releasesmetal ions and permits aggregation and coalescence of the resin andcolorant particles, resulting in formation of toner particles of fromabout 2 to about 25 microns, such as from about 3 to about 15 microns,in volume average diameter. The geometric size distribution of theresultant particles can, in embodiments, be less than about 1.40 or lessthan about 1.25, such as from about 1.15 to about 1.40.

Preferably, in embodiments, the polyion coagulant is added to themixture before the mixture is heated to cause aggregation andcoalescence of the resin and colorant dispersions. For example, thepolyion coagulant can be added to the mixture at any time beforeheating, such as during mixing of the individual components to form amixture or after the individual components are mixed together, but priorto heating. Alternatively, the polyion coagulant can be added during theheating process, such as concurrent with or after starting of theheating process, although it is preferred that the polyion coagulant isadded before the final aggregation/coalescence temperature is reached.If desired, the polyion coagulant can be added to the mixture bothbefore and during the heating step. Also if desired, the polyioncoagulant or an additional amount of the same or different polyioncoagulant can alternatively be added during or after the heating step.

Fourth, one or more optional steps can be conducted followingaggregation of the toner particles. For example, the mixture can becooled, such as to near room temperature, and the toner product isolatedfrom the reaction medium.

In the above process, the aggregation and coalescence temperature can beat any suitable temperature, such as from about 45° C. to about 80° C.,or from about 50° C. to about 75° C.

The organic or an inorganic acid suitable for use in the process is notparticularly limited. Examples of such acids include, but are notlimited to, inorganic acids such as hydrochloric acid, nitric acid,sulfuric acid, and phosphoric acid, and organic acids such as citricacid and acetic acid.

The polyion coagulant can be added to the emulsion mixture in anysuitable and desirable amount. However, in embodiments, the polyioncoagulant is added to the emulsion mixture in an amount of from about0.05 to about 10 percent by weight, such as from about 0.1 or from about0.2 to about 1 or to about 5 percent, by weight of the amount of theresin. Amounts outside these ranges can also be used.

Toner particles formed in the foregoing processes, and modificationthereof, can be isolated by any suitable means known in the art. Forexample, isolation can be conducted by filtration, wet sieving,classification, washing, drying, or the like.

The toner particles of the present disclosure can be made to have thefollowing physical properties when no external additives are present onthe toner particles.

The toner particles can have a surface area, as measured by the wellknown BET method, of about 1.3 to about 6.5 m²/g. For example, for cyan,yellow and black toner particles, the BET surface area is less than 2m²/g, such as from about 1.4 to about 1.8 m²/g, and for magenta toner,from about 1.4 to about 6.3 m²/g.

It is also desirable to control the toner particle size and limit theamount of both fine and coarse toner particles in the toner. In anembodiment, the toner particles have a very narrow particle sizedistribution with a lower number ratio geometric standard deviation(GSD) of approximately 1.15 to approximately 1.30, or approximately lessthan 1.25. The toner particles of the present disclosure also can have asize such that the upper geometric standard deviation (GSD) by volume isin the range of from about 1.15 to about 1.30, such as from about 1.18to about 1.22, or less than 1.25. These GSD values for the tonerparticles of the present disclosure indicate that the toner particlesare made to have a very narrow particle size distribution.

Shape factor is also an important control process parameter associatedwith the toner being able to achieve optimal machine performance. Thetoner particles can have a shape factor of about 105 to about 170, suchas about 110 to about 160, SF1*a. Scanning electron microscopy (SEM) isused to determine the shape factor analysis of the toners by SEM andimage analysis (IA) is tested. The average particle shapes arequantified by employing the following shape factor (SF1*a) formula:SF1*a=100 πd²/(4A), where A is the area of the particle and d is itsmajor axis. A perfectly circular or spherical particle has a shapefactor of exactly 100. The shape factor SF1*a increases as the shapebecomes more irregular or elongated in shape with a higher surface area.In addition to measuring shape factor SF, another metric to measureparticle circularity is being used on a regular bases. This is a fastermethod to quantify the particle shape. The instrument used is anFPIA-2100 manufactured by Sysmex. For a completely circular sphere thecircularity would be 1.000. The toner particles can have circularity ofabout 0.920 to 0.990 and, such as from about 0.940 to about 0.975.

In addition to the foregoing, the toner particles of the presentdisclosure also have the following rheological and flow properties.First, the toner particles can have the following molecular weightvalues, each as determined by gel permeation chromatography (GPC) asknown in the art. The binder of the toner particles can have a weightaverage molecular weight, Mw of from about 15,000 daltons to about90,000 daltons.

Overall, the toner particles in embodiments have a weight averagemolecular weight (Mw) in the range of about 17,000 to about 60,000daltons, a number average molecular weight (Mn) of about 9,000 to about18,000 daltons, and a MWD of about 2.1 to about 10. MWD is a ratio ofthe Mw to Mn of the toner particles, and is a measure of thepolydispersity, or width, of the polymer. For cyan and yellow toners,the toner particles in embodiments can exhibit a weight averagemolecular weight (Mw) of about 22,000 to about 38,000 daltons, a numberaverage molecular weight (Mn) of about 9,000 to about 13,000 daltons,and a MWD of about 2.2 to about 10. For black and magenta, the tonerparticles in embodiments can exhibit a weight average molecular weight(Mw) of about 22,000 to about 38,000 daltons, a number average molecularweight (Mn) of about 9,000 to about 13,000 daltons, and a MWD of about2.2 to about 10.

Further, the toners if desired can have a specified relationship betweenthe molecular weight of the latex binder and the molecular weight of thetoner particles obtained following the emulsion aggregation procedure.As understood in the art, the binder undergoes crosslinking duringprocessing, and the extent of crosslinking can be controlled during theprocess. The relationship can best be seen with respect to the molecularpeak values for the binder. Molecular peak is the value that representsthe highest peak of the weight average molecular weight. In the presentdisclosure, the binder can have a molecular peak (Mp) in the range offrom about 22,000 to about 30,000 daltons, such as from about 22,500 toabout 29,000 daltons. The toner particles prepared from such binder alsoexhibit a high molecular peak, for example of about 23,000 to about32,000, such as about 23,500 to about 31,500 daltons, indicating thatthe molecular peak is driven by the properties of the binder rather thananother component such as the colorant.

Another property of the toners of the present disclosure is thecohesivity of the particles prior to inclusion of any externaladditives. The greater the cohesivity, the less the toner particles areable to flow. The cohesivity of the toner particles, prior to inclusionof any external additives, may be from, for example, about 55 to about98% for all colors of the toner. Cohesivity was measured by placing aknown mass of toner, two grams, on top of a set of three screens, forexample with screen meshes of 53 microns, 45 microns, and 38 microns inorder from top to bottom, and vibrating the screens and toner for afixed time at a fixed vibration amplitude, for example for 90 seconds ata 1 millimeter vibration amplitude. A device to perform this measurementis a Hosokawa Powders Tester, available from Micron Powders Systems. Thetoner cohesion value is related to the amount of toner remaining on eachof the screens at the end of the time, and is calculated by the formula:% cohesion=50*A+30*B+10*C, where A, B and C are respectively the weightof the toner remaining on the 53 microns, 45 microns, and 38 micronsscreens, respectively. A cohesion value of 100% corresponds to all ofthe toner remaining on the top screen at the end of the vibration stepand a cohesion value of zero corresponds to all of the toner passingthrough all three screens, that is, no toner remaining on any of thethree screens at the end of the vibration step. The higher the cohesionvalue, the lesser the flowability of the toner.

Finally, the toner particles in embodiments have a bulk density of fromabout 0.22 to about 0.34 g/cc and a compressibility of from about 33 toabout 51.

The toner particles can be blended with external additives followingformation. Any suitable surface additives may be used in embodiments.Most suitable are one or more of SiO₂, metal oxides such as, forexample, TiO₂ and aluminum oxide, and a lubricating agent such as, forexample, a metal salt of a fatty acid (e.g., zinc stearate (ZnSt),calcium stearate) or long chain alcohols such as UNILIN 700, as externalsurface additives. In general, silica is applied to the toner surfacefor toner flow, tribo enhancement, admix control, improved developmentand transfer stability and higher toner blocking temperature. TiO₂ isapplied for improved relative humidity (RH) stability, tribo control andimproved development and transfer stability. Zinc stearate is optionallyalso used as an external additive for the toners of the disclosure, thezinc stearate providing lubricating properties. Zinc stearate providesdeveloper conductivity and tribo enhancement, both due to itslubricating nature. In addition, zinc stearate enables higher tonercharge and charge stability by increasing the number of contacts betweentoner and carrier particles. Calcium stearate and magnesium stearateprovide similar functions. In embodiments, a commercially available zincstearate known as Zinc Stearate L, obtained from Ferro Corporation, canbe used. The external surface additives can be used with or without acoating.

A particular advantage of embodiments is that the above externaladditives, or others, can be added to the aggregated toner particles andeffectively form a thin shell on the toner particles. Because largeramounts of the coagulant remains as part of the toner particles, thecoagulant species provide sites for increased attachment of the externaladditives to the aggregated particles. This increased attachment canresult in formation of a shell around the toner particles, not possiblewith previously known coagulant materials.

In embodiments, the toners contain from, for example, about 0.1 to about5 weight percent titania, about 0.1 to about 8 weight percent silica andabout 0.1 to about 4 weight percent zinc stearate.

The toner particles of the disclosure can optionally be formulated intoa developer composition by mixing the toner particles with carrierparticles. Illustrative examples of carrier particles that can beselected for mixing with the toner composition prepared in accordancewith the present disclosure include those particles that are capable oftriboelectrically obtaining a charge of opposite polarity to that of thetoner particles. Accordingly, in one embodiment the carrier particlesmay be selected so as to be of a negative polarity in order that thetoner particles that are positively charged will adhere to and surroundthe carrier particles. Illustrative examples of such carrier particlesinclude iron, iron alloys, steel, nickel, iron ferrites, includingferrites that incorporate strontium, magnesium, manganese, copper, zinc,and the like, magnetites, and the like. Additionally, there can beselected as carrier particles nickel berry carriers as disclosed in U.S.Pat. No. 3,847,604, the entire disclosure of which is totallyincorporated herein by reference, comprised of nodular carrier beads ofnickel, characterized by surfaces of reoccurring recesses andprotrusions thereby providing particles with a relatively large externalarea. Other carriers are disclosed in U.S. Pat. Nos. 4,937,166 and4,935,326, the disclosures of which are totally incorporated herein byreference.

The selected carrier particles can be used with or without a coating,the coating generally being comprised of acrylic and methacrylicpolymers, such as methyl methacrylate, acrylic and methacryliccopolymers with fluoropolymers or with monoalkyl or dialkylamines,fluoropolymers, polyolefins, polystyrenes, such as polyvinylidenefluoride resins, terpolymers of styrene, methyl methacrylate, and asilane, such as triethoxy silane, tetrafluoroethylenes, other knowncoatings and the like.

The carrier particles can be mixed with the toner particles in varioussuitable combinations. The toner concentration is usually about 2% toabout 10% by weight of toner and about 90% to about 98% by weight ofcarrier. However, one skilled in the art will recognize that differenttoner and carrier percentages may be used to achieve a developercomposition with desired characteristics.

Toners of the present disclosure can be used in knownelectrostatographic imaging methods. Thus for example, the toners ordevelopers of the disclosure can be charged, e.g., triboelectrically,and applied to an oppositely charged latent image on an imaging membersuch as a photoreceptor or ionographic receiver. The resultant tonerimage can then be transferred, either directly or via an intermediatetransport member, to a support such as paper or a transparency sheet.The toner image can then be fused to the support by application of heatand/or pressure, for example with a heated fuser roll.

It is envisioned that the toners of the present disclosure may be usedin any suitable procedure for forming an image with a toner, includingin applications other than xerographic applications.

Specific embodiments of the disclosure will now be described in detail.These Examples are intended to be illustrative, and the disclosure isnot limited to the materials, conditions, or process parameters setforth in these embodiments. All parts and percentages are by weightunless otherwise indicated.

EXAMPLES

Resin Emulsion A:

A sulfonated polyester resin emulsion is prepared as follows.

A sulfonated polyester resin containing 3.75 moles of sulfonation isprepared by a polycondensation reaction. The resin is ground into powderby milling. To 4400 mL of water in a reactor, is added 12.0 g NEOGEN RK®(anionic surfactant) and 8.2 g CA 897 (nonionic surfactant) and stirredat a speed of 500 rpm with a pitch blade turbine until dissolved. Tothis mixture is added 616 g of polyester resin powder, and thetemperature of the reactor is raised to 85° C. and allowed to stir for aperiod of 4 hours in order to dissipate the resin into an emulsioncontaining about 36 nm sulfonated polyester resin particles suspended inwater. The reactor is then cooled down to room temperature, and theemulsion discharged. The emulsion contains 14.0 weight percent resin and86.0 weight percent water.

Resin Emulsion B:

A sulfonated polyester resin emulsion is prepared as follows.

A sulfonated polyester resin containing 3.75 moles of sulfonation isprepared by a polycondensation reaction. The resin is ground into powderby milling. To 2000 mL of water in a reactor, is added 5.45 g NEOGEN RK®(anionic surfactant) and 1.9 g CA 897 (nonionic surfactant) and stirredat a speed of 500 rpm with a pitch blade turbine until dissolved. Tothis mixture is added 280 g of polyester resin powder, and thetemperature of the reactor is raised to 80° C. and allowed to stir for aperiod of 4 hours in order to dissipate the resin into an emulsioncontaining about 45 nm sulfonated polyester resin particles suspended inwater. The reactor is then cooled down to room temperature, and theemulsion discharged. The emulsion contains 14.0 weight percent resin and86.0 weight percent water.

Pigment Dispersion:

A pigment dispersion of an aqueous dispersion of Blue 15.3 pigment,obtained from Sun Chemicals, is used. The pigment dispersion contains ananionic surfactant. The content of the pigment dispersion is 26.5percent pigment, 2 percent surfactant, and 71.5 percent water.

Example 1

A toner is prepared as follows. To 350 g deionized water is added 687 gof the polyester resin A and 14.3 g of the colorant dispersion in a 2 Lglass reactor. To the mixture is added 3.0 g PAC (polyaluminum chloride)and 30 g of 0.1M nitric acid while being polytroned with an IKAhomogenizer at a speed of 4000 rpm. The mixture is stirred and heated toa temperature of 62° C. The particle growth is monitored during theheat-up step. The particle size obtained is 4.3 microns with a GSD of1.19.

The reactor temperature is next raised to 64° C. and allowed to stir for4 hours. The result is particles having a particle size of 7.4 micronsand a GSD of 1.17. The particles have a circular shape having acircularity of 0.978. The particles are washed 4 times with deionizedwater and dried on a freeze drier.

The thus formed toner composition is tested for its charging properties.

Comparative Example 1

A toner composition is made as in Example 1, except that the coagulantzinc acetate is used instead of polyaluminum chloride. The formed tonerparticles are similar in size and properties to those of Example 1, andhave similar charging properties.

Example 2

A toner composition is made as in Example 1, except that the coagulantused is 4.0 g polyaluminum chloride, and the aggregation temperature is62° C.

Example 3

A toner composition is made as in Example 1, except that the resin latexused is latex emulsion B. The resultant toner particles have a particlesize of 5.0 microns and a GSD of 1.19.

It will be appreciated that various of the above-disclosed and otherfeatures and functions, or alternatives thereof, may be desirablycombined into many other different systems or applications. Also thatvarious presently unforeseen or unanticipated alternatives,modifications, variations or improvements therein may be subsequentlymade by those skilled in the art which are also intended to beencompassed by the following claims.

1. A toner comprising particles of a resin, a colorant, an optional wax,and a polyion coagulant, wherein said toner is prepared by an emulsionaggregation process.
 2. The toner of claim 1, wherein the resin is apolyester resin.
 3. The toner of claim 1, wherein the polyester resin isselected from the group consisting of polyethylene-terephthalate,polypropylene-terephthalate, polybutylene-terephthalate,polypentylene-terephthalate, polyhexalene-terephthalate,polyheptadene-terephthalate, polyoctalene-terephnhalate,polyethhylene-sebacate, polypropylene sebacate, polybutylene-sebacate,polyethylene-adipate, polypropylene-adipate, polybutylene-adipate,polypentylene-adipate, polyhexalene-adipate, polyheptadene-adipate,polyoctalene-adipate, polyethylene-glutarate, polypropylene-glutarate,polybutylene-glutarate, polypentylene-glutarate, polyhexalene-glutarate,polyheptadene-glutarate, polyoctalene-glutarate polyethylene-pimelate,polypropylene-pimelate, polybutylene-pimelate, polypentylene-pimelate,polyhexalene-pimelate, polyheptadene-pimelate, poly(propoxylatedbisphenol-fumarate), poly(propoxylated bisphenol-succinate),poly(propoxylated bisphenol-adipate), poly(propoxylatedbisphenol-glutarate), sulfonated forms of the preceding resins, andmixtures thereof.
 4. The toner of claim 1, wherein the polyester resinis a sulfonated polyester resin.
 5. The toner of claim 1, furthercomprising a wax.
 6. The toner of claim 1, wherein the polyion coagulantis a metal salt or a metal oxide, the metal having a valance of at least3.
 7. The toner of claim 1, wherein the polyion coagulant is selectedfrom the group consisting of polyaluminum halides, polyaluminumsilicates, polyaluminum hydroxides, and polyaluminum phosphate.
 8. Thetoner of claim 1, wherein the polyion coagulant is selected from thegroup consisting of polyaluminum chloride and polyaluminumsulfosilicate.
 9. The toner of claim 1, wherein the polyion coagulant ispresent in the toner particles, exclusive of any optional externaladditives, and on a dry weight basis, in an amount of from less thanabout 5% by weight of the toner particles.
 10. A process for preparing atoner, comprising: mixing a resin emulsion, a colorant dispersion, andan optional wax to form a mixture; adding an organic or an inorganicacid to said mixture; adding a polyion coagulant to said mixture;heating the mixture, permitting aggregation and coalescence of saidresin and colorant, and optionally cooling the mixture and isolating theproduct, wherein the polyion coagulant is added to said mixture at leastone of before or during said heating.
 11. The process of claim 10,wherein the resin is a polyester resin.
 12. The process of claim 10,wherein the polyester resin is selected from the group consisting ofpolyethylene-terephthalate, polypropylene-terephthalate,polybutylene-terephthalate, polypentylene-terephthalate,polyhexalene-terephthalate, polyheptadene-terephthalate,polyoctalene-terephthalate, polyethylene-sebacate, polypropylenesebacate, polybutylene-sebacate, polyethylene-adipate,polypropylene-adipate, polybutylene-adipate, polypentylene-adipate,polyhexalene-adipate, polyheptadene-adipate, polyoctalene-adipate,polyethylene-glutarate, polypropylene-glutarate, polybutylene-glutarate,polypentylene-glutarate, polyhexalene-glutarate,polyheptadene-glutarate, polyoctalene-glutarate polyethylene-pimelate,polypropylene-pimelate, polybutylene-pimelate, polypentylene-pimelate,polyhexalene-pimelate, polyheptadene-pimelate, poly(propoxylatedbisphenol-fumarate), poly(propoxylated bisphenol-succinate),poly(propoxylated bisphenol-adipate), poly(propoxylatedbisphenol-glutarate), sulfonated forms of the preceding resins, andmixtures thereof.
 13. The process of claim 10, wherein the polyesterresin is a sulfonated polyester resin.
 14. The process of claim 10,further comprising mixing a wax with said resin emulsion.
 15. Theprocess of claim 10, wherein the polyion coagulant is a metal salt or ametal oxide, the metal having a valance of at least
 3. 16. The processof claim 10, wherein the polyion coagulant is selected from the groupconsisting of polyaluminum halides, polyaluminum silicates, polyaluminumhydroxides, and polyaluminum phosphate.
 17. The process of claim 10,wherein the polyion coagulant is selected from the group consisting ofpolyaluminum chloride and polyaluminum sulfosilicate.
 18. The process ofclaim 10, wherein the polyion coagulant is present in an amount of fromabout 0.05 to about 10 percent by weight of the amount of the resin. 19.The process of claim 10, wherein the polyion coagulant is added to saidmixture before said heating.
 20. The process of claim 10, wherein thepolyion coagulant is added to said mixture during said heating.
 21. Theprocess of claim 10, wherein the polyion coagulant is added to saidmixture both before and during said heating.
 22. The process of claim10, wherein the organic or an inorganic acid is selected from the groupconsisting of hydrochloric acid, nitric acid, sulfuric acid, phosphoricacid, citric acid, and acetic acid.
 23. The process of claim 10, furthercomprising adding at least one surfactant to said resin emulsion. 24.The process of claim 10, wherein at least about 75% by weight of thepolyion coagulant is incorporated into the toner particles duringparticle aggregation.
 25. A developer comprising: the toner of claim 1,and a carrier.
 26. An electrographic image development device,comprising the toner of claim 1.